2-substituted amino-5-phenyl-3h-1 4-benzodiazepines

ABSTRACT

3H-1,4-BENZODIAZEPINES OF THE FORMULA II:   2-(R-O-NH-),5-(R3,R4-PHENYL),R1,R2-3H-1,4-BENZODIAZEPINE   WHEREIN R IS SELECTED FROM THE GROUP CONSISTING OF HYDROGEN, LOWER-ALKYL OF 1 TO 4 CARBON ATOMS, INCLUSIVE, ALKENYL OF 3 OR 4 CARBON ATOMS, BENZYL, -CH2-COOH AND -(CH2)2-COOH AND THE ESTERS THEREOF DERIVED FROM AN ALKANOL OF 1 TO 3 CARBON ATOMS, INCLUSIVE, AND   -(CH2)N-N(-R5)-R6   IN WHICH N IS 2 OR 3 AND R5 AND R6 ARE LOWER-ALKYL OF 1 TO 4 CARBON ATOMS, INCLUSIVE, OR R5 AND R6 TOGETHER ARE ALKYLENE OF 4 OR 5 CARBON ATOMS; AND WHEREIN R1, R2, R3 AND R4 ARE SELECTED FROM THE GROUP CONSISTING OF HYDROGEN, ALKYL DEFINED AS ABOVE, THIOALKYL IN WHICH ALKYL IS DEFINED AS ABOVE, LOWER ALKOXY OF 1 TO 3 CARBON ATOMS, INCLUSIVE, HALOGEN, NITRO, CYANO AND -CF3; ARE PREPARED BY CONDENSING THE CORRESPONDING THIOLACTAM COMPOUND I:   2-(S=),5-(R3,R4-PHENYL),R1,R2-1,2-DIHYDRO-   3H-1,4-BENZODIAZEPINE   WITH A COMPOUND OF THE FORMULA H2N-OR IN WHICH R IS DEFINED AS ABOVE. THESE COMPOUNDS AND THEIR PHARMACOLOGICALLY ACCEPTABLE ACID ADDITION SALTS HAVE SEDATIVE AND TRANQUILIZING ACTION AND CAN BE USED IN MAMMALS AND BIRDS AS TRANQUILIZERS.

r 3,649,617 Patented Mar. 14, 1972 United States Pate BACKGROUND OF THE INVENTION 3 649 617 Z-SUBSTITUTED AfMINO-S-PHENYLH-IA- Fleld of the mventlon BENZODIAZEPINES This invention is directed to new organic compounds Jackson golmgfiester Galesbmg Mich" I'sslgnor m and is particularly concerned with novel 3H-1,4-benzo- No g s a i l gg fig fgzi fi 3; ggggggg er Na diazepines and a process for the production thereof.

803,450, Feb. 28, 1969. This application July 20, 1970, gfi the g s firodactwn S r, N 56,750 t ere or can e 1 ustrative y represente as o ows.

Int. Cl. C0711 29/28, 53/06 s NH OR U.S. Cl. 260-239 BD 13 Claims H I My. a. w .H N R1 HEN-OR HS ABSTRACT OF THE DISCLOSURE mi 1 3 R2 3H-1,4-benzodiazepines of the Formula II: W

BITE-OR N= R3 R, /9\/ [8 1 2 R, I R4 Eli 3 I H 2 W 5 4 wherein R is selected from the group consisting of hydro- W N gen, alkyl of 1 to 4 carbon atoms, inclusive, alkenyl of 3 or 4 carbon atoms, benzyl, CH COOH and R (CH COOH and the esters thereof derived from an R4 alkanol with 1 to 3 carbon atoms, inclusvie, and II R wherein R is selected from the group consisting of hydro- OH N 5 gen, lower-alkyl of 1 to 4 carbon atoms, inclusive, alkenyl 2)- of 3 or 4 carbon atoms, benzyl, CH -COOH and Re ggigig z zi g g s fis g gfgig iz from in which n is 2 or 3 and R and R are lower-alkyl of 1 to 4 carbon atoms, inclusive, or R or R together are alkylene of 4 to 5 carbon atoms; and wherein R R (OH2)nN R and R are selected from the group consisting of hydrogen, alkyl defined as above, thioalkyl in which the alkyl group is defined as above, alkoxy of 1 to 3 carbon in which n is 2 or 3 and R and R are lower-alkyl of 1 to atoms, inclusive, halogen, nitro Cyano and 4 Carbon atoms mcluslve or R5 and R6 .together are The process of this invention comprises heating a thio alkylene of 4 or 5 Car atoms; and w f R3 lactam of Formula I above with an oxylamine H N-OR and R are selected from the group consisting of hydrogen, in which R is defined as above in an organic Solvent or alkyl defined as above, thioalkyl in which alkyl is defined suspending agent to about 604300 C for 2 to 18 hours as above, lower alkoxy of 1 to 3 carbon atoms, inclusive,

halogen, nitro, cyano and CF;;; are prepared by con- DESCRIPTION OF THE PREFERRED densing the corresponding thiolactam Compound I: EMBODIMENT H S Lower-alkyl groups of 1 to 4 carbon atoms, inclusive, /9\/ are exemplified by methyl, ethyl, propyl, isopropyl, butyl, |s 1 sec.-butyl, isobutyl and tert.-butyl. 1 I 3 Examples fo alkenyl of 3 to 4 carbon atoms are allyl, 2 7 I Z-methylallyl, 2-butenyl (crotyl), 3-butenyl and the like.

5 1 Examples of the radical 5 (3:11;, (CH2)QN R4 R5 I with a compound of the formula H NOR in which R is 2'(cilmqthylanfimio)ethyi 2 1(1d1eth1amm0ethy1) defined as above. These compounds and their pharmaco- 1p mp y ammmet y 3% ylammo)propyl 3-1) 1- logically acceptable acid addition salts have sedative and periqinopmpyl Z'pyrrolidinoethyl z-piperidinoethyl and tranquilizing action and can be used in mammals and birds the as tranquilizers The term halogen for R R R and R means fluoro,

6O chloro and bromo.

. The novel compounds of the Formula II including CROSS REFERENCES To, RELATED pharmacologically acceptable acid addition salts thereof APPLICATION lga e sedative and tranquilizing effects in mammals and it s.

This application is a continuation-in-part of application The pharmacologically acceptable acid addition salts of Ser. No. 803,450, filed Feb. 28, 1969 and now abandoned. compounds of Formula II contemplated in this invention 3 are the hydrochlorides, hydrobromides, hydriodides, sulfates, phosphates, acetates, lactates, tartrates, citrates, salicylates, succinates, malates, maleates, pamoates, cyclohexanesulfamates, methanesulfonates and the like, prepared by reacting a compound of Formula II with the stoichiometrically calculated amount of the selected pharmacologically acceptable acid.

Illustratively, sedative eifects of 2-(methoxyamino)-7- chloro-5-phenyl-3H-1,4-benzodiazepine are shown by the following tests in mice:

Chimney test [Merl Exp. 4, 11 (1961)]: The effective intraperitoneal dosage for 50% of mice, ED is 28 mg./ kg. The test determines the ability of mice to back up and out of a vertical glass cylinder vw'thin 30 seconds. At the effective dosage, 50% of the mice failed doing it.

Dish test: Mice in Petri dishes (10 cm. diameter, 5 cm. high, partially embedded in wood shavings), climb out in a very short time, when not treated. If mice remain in the dish for more than 3 minutes, it indicates tranquilization. ED equals the elfective dosage of test compound at which 50% of the mice remain in the dish. ED (intraperitoneal administration) in this test was 2-3 mg./kg.

Pedestal rest: The untreated mouse leaves the pedestal in less than one minute to climb back to the floor of the standard mouse box. Tranquilized mice will stay more than one minute. ED (intraperitoneal administration) was 16 trig/kg.

Nicotine antagonism test: Mice in a group of 6 were injected intraperitoneally with 2-(methoxyamino-7-chloro-5-phenyl-3H-1,4-benzodiazepine. Thirty minutes later the mice including control (untreated) mice are injected with 2 mg./kg. nicotine salicylate. The control mice show over-stimulation, i.e., (1) running convulsions followed by (2) tonic extensor fits; followed by (3) death. An intraperitoneal dosage of 2-4 mg./kg. of the test compound protected 50% or the mice against (2) and (3) (ED oral ED was 1.4 mg./kg.

The compounds, 2 [(allyloxy)amino] 7-nitro5-(ochlorophenyl) 3H 1,4 benzodiazepine (A) and 2-[(2- alloyloxyarnino 7 chloro 5 (o-chlorophenyl-3H-l,4- benzodiazepine (B) were tested in tests as described above with these results:

No'rE.Chlm.=Chlmney test; Dish=Dish test; Peri.=Pedestal test; Nlc. 2=Nicotlno antagonism-tonic extensor tits (2); N10. 3=Nieotine antagonism-death (3).

The pharmaceutical forms contemplated by this invention include pharmaceutical compositions suited for oral, parenteral and rectal use, e.g., tablets, oils, powder packets, cachets, dragees, capsules, solutions, suspensions, sterile injectable forms, suppositories, bougies, and the like. Suitable diluents or carriers such as carbohydrates (lactose), proteins, lipids, calcium phosphate, cornstarch, stearic acid, methylcellulose and the like may be used as carriers or for coating purposes. Oil, e.g., coconut oil, sesame oil, satfiower oil, cottonseed oil, peanut oil may be used for preparing solutions or suspensions of the active drug. sweetening, coloring and flavoring agents may be added.

For mammals and birds food premixes, with starch, oatmeal, dried fishmeal, fishmeal, flour and the like can be prepared.

As tranquilizer the compounds of Formula II can be used in dosages of 1-50 rug/kg. in oral or injectable preparations as described above, to alleviate tension and anxiety in mammals or birds, such as, e.g., occurs when animals are in travel.

Other acid addition salts of the compounds of Formula II can be made such as the fiuosilicic acid addition salts which are useful mothproofing compounds or the trichloroacetates useful as herbicides against Johnson grass,

4 Bermuda grass, yellow foxtail and green foxtail, and quack grass.

Starting materials of Formula I of this invention, substituted or unsubstituted 1,3-dihydro-5-phenyl-2H-1,4- benzodiazepine-Z-thiones, and methods for their preparation, are described by G. Archer and L. H. Sternbach, J. Org. Chem. 20, 231 (1964); see also US. Pat. 3,422,091. These compounds (I) are prepared by heating substituted or unsubstituted l,3-dihydro-5-phenyl-2H-1,4- benzodiazepine-Z-ones and phosphorus pentasulfide in pyridine for about 45 minutes (Archer et al., ibid; US. Pat. 3,422,091). The following compounds of Formula I are representative starting products:

1,3-dihydro-5-phenyl-2H-1,4-benzodiazepine-2-thione;

7-chloro-1,3-dihydro-5-phenyl-2H-1,4-benzodiazepine- 2-thione;

7-bromo-1,3-dihydro-5-phenyl-2H-1,4-benzodiazepine- Z-thione;

7-methyl-1,3-dihydro-5-phenyl-2H-1,4-benzodiazepine- 2-thione;

7-nitro-1,3-dihydro-5-phenyl-2H-1,4-benzodiazepine- 2-thione;

7-trifiuoromethyll ,3-dihydro-5 -pheny1-2H- 1 ,4-

benzodiazepine-Z-thione;

7-cyano-1,3-dihydro-5-phenyl-2H-1,4-benzodiazepine- 2-thione;

7-chloro-1,3-dihydro-5-(o-chlorophenyl)-2H-1,4-

benzodiazepine-Z-thionc;

7-chloro-1,3-dihydro-5-(ofiuorophenyl)-2H-1,4-

benzodiazepine-2-thione;

7-bromo-1,3-dihydro-5-(o-fluorophenyl)-2H-l,4-

benzodiazepine-Z-thione;

7-fluoro- 1 ,3-dihydro-5- (o-fluorophenyl) -2I-I- 1,4-

benzodiazepine-Z-thione;

7-nitrol ,3-dihydro-5 (o-chlorophenyl) -2H-1,4-

benzodiazepine-Z-thione;

7-brorno-1 ,3 -dihydro-5- (o-bromophenyl -2H- 1 ,4-

benzodiazepine-Z-thione;

7-methyl-l,3-dihydro-5-(o-chlorophenyl)-2H-1,4-

benzo di azepine-Z-thione;

7-cyano-1,3-1dihydro-5-(o-chlorophenyl)-2H-l,4-

benzodiazepine-Z-thione;

T-trifiuoromethyl-1,3-dihydro-5-(o-chlorophenyl)-2H-1,4-

benzodiazepine-Z-thione;

7-fluoro-l,3-dihydro-5- (o-chlorophenyl) -2H-1,4-

benzodiazepine-Z-thione;

1,3-dil1ydro-5-(o-chlorophenyl)2H-1,4-benzodiazepine- 2-thione;

1,3-dihydro-S 2,6-dichlorophenyl) -2H-1,4-benzodiazepine-Z-thione;

1,3-dihydro-5- 2,6-difiuorophenyl) -2H- 1 ,4-benzodiazepine-2-thione;

7,9-dichloro-l,3-dihydro-5-(2,6-dichlorophenyl) 2H-1,4-

benZo diazepine-2-thione;

6,7-dicyano-1,3-dihydro-5-(m-nitropheny1)-2H-1,4-

benzo diazepine-Z-thione;

6 -methyl7-bromo- 1, 3 -dihydro- 5 (p-methylphenyl -2H- 1,4beuZodiazepine-2-thione;

7-trifiuoromethyl-8-cyano-1,3-dihydro-5-(2-chloro-5- methylphenyl) -2H- l,4-benzodiazepine-Z-thione;

7,9-dicyauo-1,3-dihydro-5- (2,4-dibromophenyl) -2H-l,4-

benzodiazepine-Z-thione;

6,8-dimethyl-1,3-dihydro-5-(3 ,S-diethoxyphenyl -2H- 1 ,4-benzodiazepine-2-thione;

and the like.

In carrying out the process of the invention, a selected l,3-dihydro-5-phenyl-2H-1,4benzodiazepine-2-thione (I), an oxyamine of formula H NO-R in which R is defined as above, usually in the form of a salt such as hydrochloride or hydrobromide, a base e.g. carbonate, bicarbonate, or hydroxides of alkali metals to absorb the acid moiety of the oxyamine salt and a solvent are refluxed for a period of 2-18 hours. In the preferred embodiment of this invention, the organic solvent used may be methanol, ethanol, 2-propanol, or such co-solvents as methanol-dimethyl sulfoxide, or the like. The oxyamine is usually used in excess, such as from 1.5 to times the molar equivalent of the thione starting material. The base is used in sufficient quantity to produce the oxyamine in the free base state. After the reaction is terminated, the mixture is filtered, the filtrate concentrated in vacuo and the product obtained by standard procedures such as extraction, crystallization, recrystallization and chromatography to give the pure product, a 2-(oxyamino)-5-phenyl-3H-1,4-benzodiazepine of Formula II.

The following examples are illustrative of the processes and products of the present invention, but are not to be construed as limiting.

EXAMPLE 1 2- (methoxyamino)-7-clzl0r0-5-phenyl-3H-1,4-benz0- diazepine A mixture of 45.6 g. (0.160 mole) of 7-chloro-1,3-dihydro-5-pheny1-2H-1,4-benzodiazepine-2-thione, 26.7 g. of methoxyamine hydrochloride, 26.9 g. of sodium bicarbonate and 800 ml. of methanol was refluxed under nitrogen for 5.5 hours, cooled and filtered. The filtrate was concentrated in vacuo to give a residue. A solution of the residue in methylene chloride was absorbed on a 3 kg. silica gel column which had been prepared with methylene chloride. The column was then eluted with 30% ethyl acetate-70% cyclohexane; 400 ml. fractions were collected. Unreacted starting material was eluted in fractions -32. The product was eluted in fractions 42-85 and was crystallized from ethyl acetate to give 29.8 g. (62.3%) of 2- (methoxyamino) 7 chloro 5 phenyl-3H-1,4-benzo diazepine of melting point 184.5-186 C. The analytical sample of melting point 185-186 C. was prepared recrystallizing this material from methanol. The ultraviolet spectrum (ethanol) had r 212, 253 and 343 m (E: 33,800, 26,850 and 2,850, respectively) and an inflection at 227 In, 25,950).

Analysis.Calcd. for C H CIN O (percent): C, 64.11; H, 4.71; Cl, 11.83; N, 14.02. Found (percent): C, 63.84; H, 4.71; Cl, 12.17; N, 13.91.

EXAMPLE 2 2-(benzyloxyamilzo)-7-chl0r0-5-plze11yl-31I-J,4-benz0- diazepine A mixture of 1.43 g. (0.005 mole) of 7-chloro-1,3-dihydro-5-phenyl-2H-1,4-benzodiazepine 2 thione, 1.60 g. (0.01 mole) of benzyloxyamine hydrochloride, 0.84 g. (0.01 mole) sodium bicarbonate and 50 ml. of methanol was refluxed for 10 hours, cooled and filtered. The solid was recrystallized from methanol to give 1.02 g. (54%) of 2 (benzyloxyamino)-7-chloro-5-phenyl-3H-1,4-benzodiazepine of melting point 178-181.5 C. The analytical sample, melting point 180181.5 C., was prepared by recrystallizing this material from methanol. The ultraviolet spectrum (ethanol) had a k 209, 254 and 343 m (e=33,l00, 28,800 and 1,950, respectively) with an inflection at 230 111 1. (e=26,450).

Analysis.-Calcd. for C H ClN O (percent): C, 70.30; H, 4.85; Cl, 9.43; N, 11.18. Found (percent): C, 70.12; H, 5.06; Cl, 9.46; N, 11.32.

EXAMPLE 3 2- [2- (I-pyrrolizlinyl) ethoxyamz'no] 7-chl0r0-5-phenyl- 3H-l,4-benz0diazepine and hydrate thereof A mixture of 2.87 g. (0.01 mole) of 7-chloro-1,3-dihydro 5 phenyl-2H4,4benzodiazepine-Z-thione, 4.06 g. (0.02 mole) of 2-(l-pyrrolidinyl)ethoxyamine dihydrochloride, 3.36 g. (0.04 mole) of sodium bicarbonate and 100 ml. of methanol was refluxed under nitrogen for 2 hours, cooled and filtered. The filtrate was concentrated in vacuo and the thus-obtained residue was crystallized from ethyl acetate to give 1.69 g. (44.3%) of 2-[2-1-pyrrolidinyl)ethoxyamino]-7-chloro 5 phenyl 3H 1,4- benzodiazepine as hydrate, of melting point 122.5-130" C. The analytical sample of melting point 137.5-138.5 C. was prepared by recrystallizing some of this material from ethyl acetate. The ultraviolet spectrum (ethanol) had Amax. 212, 254 and 345 111,11. (e=32,100, 25,850 and 1,950, respectively) with an inflection at 228 m (e=24,650).

Arzalysi.r.-Calcd. for C H ClN O-H O (percent): C, 62.91; H, 6.29; CI, 8.85; N, 13.98; E 0, 4.49. Found (percent): C, 63.19; H, 6.24; Cl, 9.22; N, 13.57; H O, 3.54.

Heating this hydrate to 110 C. for 72 hours at 15 mm. Hg pressure gave water-free 2-[2-(1-pyrrolidinyl)ethoxyamino] -7-chloro-5-phenyl-3H1,4-benzodiazepine.

EXAMPLE 4 2-( butoxyamino)-7-chl0r0-5-phenyl-3H-1,4-benzodiazepine A mixture of 1.43 g. (0.005 mole) of 7-chloro-1,3-dihydro-5-phenyl-2H-1,4-benzodiazepine 2 thione, 1.26 g. (0.01 mole of t-butoxyamine hydrochloride, 0.85 g. (0.01 mole) of sodium bicarbonate and 50 ml. of methanol was refluxed under nitrogen for 6 hours. At this time very little reaction could be detected by thin layer chromatography. Dimethyl sulfoxide (5 ml.) was added, and this mixture was refluxed for 7 hours, cooled and filtered. The resulting solid was recrystallized from ethyl acetate to give 0.24 g. (14%) of 2-(t-butoxyamino) 7 chloro-5- phenyl-3H-1,4-benzodiazepine of melting point 252 C. (dec.). The analytical sample of melting point 251.5-252 C. (dec.) was prepared by recrystallzing this material from ethyl acetate. The ultraviolet spectrum (ethanol) had A 212, 254 and 346 m (e=35,400, 24,850 and 1,900 respectively).

Analysis.-Calcd. for C H ClN O (percent): C, 66.76; H, 5.90; Cl, 10.37; H, 12.29. Found (percent): C, 66.77; H, 5.94; Cl, 10.66; N, 12.29.

EXAMPLE 5 2- (allyloxyamino -7-chl0r0-5-ph enyl-3H-1 ,4: benzodiazepine A mixture of 2.87 g. (0.01 mole) of 7-chloro-1,3-dihydro 5-phenyl-2H-1,4-benzodiazepine-Z-thione, allyloxyamine hydrochloride (2.20 g.; 0.02 mole), sodium bicarbonate (1.77 g.; 0.021 mole) and absolute ethanol was refluxed for 4.5 hours with a slow stream of nitrogen bubbling through the reaction mixture. The reaction mixture was cooled and filtered, the filtrate was concentrated in vacuo and the residue was chromatographed on silica gel (300 g.) with 10% ethyl acetate-% methylene chloride; -ml. fractions were collected. The product was eluted in fractions 30-62 and crystallized from ether- Skellysolve B hexanes to give 1.19 g. of 2-(allyloxyamino)-7-chloro-5-phenyl-3H-1,4-benzodiazepine of melting point 126.5-129" 'C. The analytical sample had a melting point of 134135.5 C. The ultraviolet spectrum (ethanol) had A 211 (e=34,550), 254 (e=27,350), 343 (e=1,850), inflection 229 m (e=25,900).

Analysis.Calcd. for C H ClN o (percent): C, 66.36; H, 4.95; Cl, 10.88; N, 12.90. Found (percent): C, 66.20; H, 4.95; Cl, 11.12; N, 12.43.

EXAMPLE 6 2-[Z-(diethylamino)ethoxyamino]-7-chl0r0-5-pl1enyl 3H-L4-benz0diazepine and hem'ihydrafe thereof A mixture of 4.3 g. (0.015 mole) of 7-chloro-1,3-dihydro S-phenyl-ZH-l,4-benzodiazepine-Z-thione, 2-(diethylamino)ethoxyamine (3.96 g.; 0.030 mole) and absolute ethanol ml.) was refluxed, under nitrogen, for 7 hours and concentrated in vacuo. The residue was crystallized from ethyl acetate-Skellysolve B hexanes to give 5.25 g. (91%) of 2-[2-(diethylamino)ethoxyamino]- 7-chloro-5-phenyl-3H-1,4-benzodiazepine as hemihydrate of melting point 92-100 C. The analytical sample had a melting point of 99-100 C. The ultraviolet spectrum (ethanol) had A 211 (e=33,850), 254 (e=25,650), 344 (e=2,000), inflection 227 m (e=25,600).

Analysis.-Calcd. for C H C1N O,.1/2H O (percent): C, 64.03; H, 6.65; CI, 9.00; N, 14.22. Found (percent): C, 63.93; H, 6.60; Cl, 9.02; N, 13.85.

Heating this hydrate to 80 C. for 72 hours at 15 mm. Hg pressure gave water-free 2-[2-(diethylamino)ethoxyamino] -7-chloro-5-phenyl-3H-1,4-benzodiazepine.

EXAMPLE 7 Ethyl (7-chloro-5-phenyl-3H-1,4-benz0diazepin- Z-yl) aminooxy] acetate A mixture of 11.5 g. (0.04 mole) of 7-chloro-l,3-di hydro 5 phenyl-2H-1,4-benzodiazepine-2-thione, ethyl aminooxyacetate (11.9 g.; 0.10 mole), dimethyl sulfoxide (40 ml.) and absolute ethanol (400 ml.) was refluxed for 7 hours with a stream of nitrogen bubbling through the mixture. Additional ethyl aminooxyacetate (6.0 g.) was added to the mixture which was refluxed for an additional 18 hours and concentrated in vacuo. The residue was suspended in water and the mixture was extracted with ether. The ether extract was dried over anhydrous potassium carbonate and concentrated to give a residue. The residue was chromatographed on silica gel (750 g.) with 25% ethyl acetate-75% cyclohexane; ZOO-ml. fractions were collected. The product of fractions 30-56 was crystallized from ether-Skellysolve B hexanes to give 2.59 g. of melting point 116-117 C. and 2.07 g. of melting point l13-.115.5 C. of ethyl [(7-ch1oro-5-phenyl3H-1,4- benzodiazepin 2 yl)aminooxy]acetate. The analytical sample had a melting point of 113-1 14 C. The ultraviolet spectrum (ethanol) had k i 210 (e=34,560, 252 (e=28,150), 341 (e=2,050), inflection 228 mp. (E=26,300)- Analysis.-Calcd. for C H ClN O (percent): C, 61.37; H, 4.88; Cl, 9.54; N, 11.30. Found (percent): C, 61.48; H, 5.14; Cl, 9.55; N, 11.17.

EXAMPLE 8 2- (hydroxyamino)-7-chl0r0-5-phenyl-3H-I,4- benzodiazepine A mixture of 14.4 g. (0.05 mole) of 7-chloro-l,3-dihydro-S-phenyl-ZH-l,4-benzodiazepine-2-thione, hydroxylamine hydrochloride (4.55 g.), sodium bicarbonate (5.45 g.) and methanol (250 ml.) was refluxed for 1.5 hours with a stream of nitrogen bubbling through the mixture. The cooled mixture was filtered and the filtrate was concentrated in vacuo to give a residue. This residue was chromatographed on silica gel (750 g.); 150-ml. fractions were collected. The product was eluted with 2% triethylamine-13% methanol-85% ethyl acetate and crystallized from ethyl acetate to give 4.92 g. of melting point 122.5-130" C. and 3.38 g. of melting point 128- 132 C. of 2-(hydroxyamino)-7-chloro-5-phenyl-3H-1,4- benzodiazepine. The analytical sample had a melting point of 126130 C. The ultraviolet spectrum (ethanol) had A 209 (e=34,050), 252 (e=23,750), 345 (e=l,800), inflection 229 mu (s=24,250).

Analysis.Calcd. for C H ClN O (percent): C, 63.05; H, 4.23; CI, 12.41; N, 14.71. Found (percent): C, 63.13; H, 4.40; Cl, 12.31; N, 14.52.

EXAMPLE 9 2-(allyl0xyamin0) -7-ch[or0-5- (-chl0r0phenyl)- 3H -1 ,4-benz0diaze pine A mixture of 7-chloro-l,3-dihydro-5-(o-chlorophenyl)- 2H1,4-benzodiazepine-2-thione (1.52 g., 0.005 mole), allyloxyamine hydrochloride (1.10 g., 0.01 mole), sodium bicarbonate (0.89 g., 0.011 mole) and absolute ethanol (50 ml.) was refluxed for hours with a slow stream of nitrogen bubbling through the reaction mixture. The mixture was cooled and filtered, and the filtrate was concentrated in vacuo. Crystallization of the residue from ethyl acetate gave 0.21 g. of recovered starting material, chromatographing the mother liquors on silica gel (100 g.) with 25% ethyl acetate-75% cyclohexane. Crystallization from ethyl acetate-Skellysol-ve B hexanes gave 0.68 g. (37.8%) of 2 (allyloxyamino) 7-chloro-5-(ochlorophenyl)-3H-1,4-benzodiazepine, melting point 130- 131 C. The analytical sample, melting point 130-131 C. was prepared by recrystallizing some of this material from ethyl acetate-Skellysolve B hexanes. The ultraviolet spectrum (ethanol) had A 234 and 346 mu (e=26,950 and 2,150, respectively) with inflections at 208, 253 and 275 mu (e=38.750, 21,160 and 10,750, respectively).

Analysis.-Calcd. for C H Cl N O (percent): C, 60.01; H, 4.20; CI, 19.68; N, 11.66. Found (percent): C, 59.88; H, 4.29; Cl, 19.40; N, 11.41.

EXAMPLE 10 2-(methoxyamino)-7-chl0r0-5-(o-chlorophenyl -3H-1,4-berzz0diazepine A solution of 7-chloro-l,3-dihydro-5-(o-chlorophenyD- 2H-1,4-benzodiazepine-2-thione (7.42 g., 0.0244 mole) in a mixture of 1 N sodium hydroxide solution (28.9 ml.) and methanol (36 ml.) was treated during 20 minutes with a solution of dimethyl sulfate (3.35 g.) in methanol (12 ml.). This mixture was stirred for 10 minutes, diluted with water, made strongly alkaline with sodium hydroxide and extracted with ether. The extract was Washed with water, dried with anhydrous potassium carbonate and concentrated. The residue was chromatographed on silica gel (500 g.) with 25% ethyl acetate- 75% cyclohexane. The resulting product was crystallized from ether at 0 C. to give 3.71 g. of 7-chloro- Z-(methylthio) 5 (o-chlorophenyl)-3H-1,4-benzodiazepine of melting point 113-118.5 C. The analytical sample of melting point ll8120 C. was prepared by recrystallizing some of this material from methylene chloride-ether. The ultraviolet spectrum (ethanol) had 1 244 and 286 mu (e=23,600 and 11,500, respectively) with inflections at 215 and 330 m (e=30,350 and 3,650, respectively) Analysis.-Calcd. for C H Cl N S (percent): C, 57.32; H, 3.61; CI, 21.15; N, 8.36; S, 9.57. Found (percent): C, 57.82; H, 3.77; CI, 21.37; N, 8.44; S, 8.97.

A mixture of 7-chloro-2-(methylthio)-5-(o-chlorophenyl)-3H-1,-4-benzodiazepine (1.60 g.; 0.00476 mole), methoxyamine hydrochloride (0.794 g.), sodium bicarbonate (0.794 g.) and absolute ethanol ml.) was refiuxed for 4 hours with a slow stream of nitrogen flowing through the reaction mixture. This mixture was concentrated in vacuo; the residue was mixed with water and extracted with methylene chloride. The extract was washed with water, dried with anhydrous potassium carbonate and concentrated. Crystallization of the residue from ethyl acetate gave 1.11 g. of Z-methoxyamino)-7-chloro-5-(o chlorophenyl) 3H-1,4-benzodiazepine, melting point 157- 159 C. The analytical sample, melting point 158.5159.5 C. was prepared by recrystallizing this material from ethyl acetate. The ultraviolet spectrum (ethanol) had A 234 and 346 m (e=26,150 and 2,050, respectively) with inflections as 211, 253 and 275 mu (e=37,050, 19,650 and 10,200, respectively).

Analysis.Calcd. for C H Cl N O (percent): C, 57.50; H, 3.92; Cl, 21.22; N, 12.57. Found (percent): C, 57.17; H, 4.00; Cl, 21.44; N, 12.35.

EXAMPLE 11 L(7-chl0r0-5-phenyl-3H-1,4-benzodiapinc- 2-yl aminooxy] acetic acid In the manner given in Example 1, 7-chloro-l,3-dihydro-5-phenyl-2H-1,4-benzodiazepine-Z-thione and aminooxyacetic acid were refluxed methanol for 6 hours to give [(7 chloro-5-phenyl-3H-l,4-benz0diazepine-2-yl)aminooxylacetic acid.

9 EXAMPLE 12 Z-(ethoxyamino) -7-br0m0-5-phenyl-3H- 1,4-benzdiazepine In the manner given in Example 1, 7-bromo-1,3-dihydro--phenyl-2H-1,4-benzodiazepine 2 thione, ethoxyamine hydrochloride, sodium bicarbonate and methanol were refluxed for 6 hours to give 2-(ethoxyarnino)-7 bromo-S-phenyl-H-1,4-benzodiazepine.

EXAMPLE 13 Z-(butOxyamino) -7-triflu0r0methyl-5- (o-chlorophenyl )-3H-1,4-benz0diazepine In the manner given in Example 1, 7-trifluoromethyl- 1,3-dihydro-5-(o chlorophenyD-ZH-1,4-benzodiazepine- 2-thione, butoxyamine hydrochloride, sodium bicarbonate and methanol were refluxed for 6 hours to give 2- (butoxyamino)-7-trifluorornethyl-5- (o chlorophenyl-3H- 1,4-benzodiazepine.

EXAMPLE 14 2- [3-(1-pyrr0lidinyl)propoxyamino] -7-cyan0-5- (o-fluorophenyl) -3H-1,4-benzodiazepine In the manner given in Example 1, 7-cyano-l,3-dihydro-5-(o fluorophenyl)-2H-1,4-benzodiazepine-Z-thione, 3-(l-pyrrolidinyl)propoxyamine hydrochloride, sodium bicarbonate and methanol were refluxed for 6 hours to give 2-[3-(1 pyrrolidinyl)propoxyarnino1-7-cyano-5-(ofluorophenyl)-3H-1,4-benzodiazepine.

EXAMPLE l5 2- [2-(1-pz'peridinyl) ezhoxyamino] -7-nitr0-5- (a-bromophenyl) -3H-1,4-benz0diazepine In the manner given in Example 1, 7-nitro-1,3-dihydro-5-(o bromophenyl)2H-1,4-benzodiaZepine-2-thione, 2-(l-piperidinyl)ethoxyamine hydrochloride, sodium bicarbonate and methanol were refluxed for 6 hours to give 2-[2-(l-piperidinyl)ethoxyamino] 7 nitro-S-(o-bromophenyl)-3H-l,4-benzodiazepine.

EXAMPLE 16 2- (hydroxyami no -7-flu0ro-5 pheny 3H-1 ,4-benz0diazepine In the manner given in Example 1, 7-fluoro-1,3-dihydro-S-phenyl-ZH-1,4-benzodiazepine 2 thione, hydroxyamine hydrochloride, potassium bicarbonate and ethanol were refluxed for 6 hours to give 2-(hydroxyamino)-7- fluoro-5-phenyl-3H-1,4-benzodiazepine.

EXAMPLE 17 2- (crotyloxyamino)-5-phenyl-3H-1,4-benz0diazepine In the manner given in Example 1, 1,3-dihydro-5-phenyl-2H-1,4-benzodiazepine-Z-thione, crotyloxyarnine hydrochloride, sodium bicarbonate and methanol were refluxed for 6 hours to give 2-(crotyloxyamino)-5-phenyl-3H1,4 benzodiazepine.

EXAMPLE l8 2- (propoxyamino -7-methyl-5- (0flu0r0- phenyl) -3H-1,4-benz0diazepine In the manner given in Example 1, 7-methyl-1,3-dihydro-5-(o fluorophenyl)-2H-1,4-benzodiazepine-2-thione, propoxyamine hydrochloride, sodium bicarbonate and methanol were refluxed for 6 hours to give 2-(propoxyamino)-7-methyl-5-(o fluorophenyl)3H-l,4-benzodiazepine.

EXAMPLE 19' In the manner given in Example 1, 7-trifluoromethyl 1,3 -dihydro 5- (o chlorophenyl -2H- 1 ,4-b enzodiazepine- 2 thione, 3 (dimethylamino)propoxyarnine hydrochloride, sodium bicarbonate and methanol were refluxed for 6 hours to give 2-[3-(dimethylamino)propoxyamino]-7- trifluoromethyl-5- (o-chlorophenyl-3H-1,4-benzodiazepine.

EXAMPLE 20 3-[ (7-fluor0-5-phenyl-3H-1,4-benzodiazepin- 2-yl)-amin00xy] propionic acid In the manner given in Example 11, 7-fluoro-1,3-dihydro-5-phenyl-2H-1,4-benzodiazepine-Z-thione, B-(aminooxy)propionic acid and methanol were refluxed for 6 hours to give 2-[(7-fluoro-5-phenyl-3H-1,4-benzodiazepin-Z-yl)aminooxy1propionic acid.

EXAMPLE 21 Methyl 7-br0mo-5-phenyl-3H-I,4-benzodiazepin- 2-yl)amin00xy]acetate EXAMPLE 22 Z-(isobutoxyamino) -7-cyan0-5-phenyl- 3H ,4-benz0diazepine In the manner given in Example 1, 7-cyano-1,3-dihydro 5-phenyl-2H-1,4-benzodiazepine-2-thione, isobutoxyamine hydrochloride, sodium bicarbonate and methanol were refluxed for 6 hours to give 2-(isobutoxyamino)-7-cyano- 5-phenyl-3H-1,4-benzodiazepine.

EXAMPLE 23 2-[ (allyloxy amino] -7-nitr0-5- (o-chlorophenyl) 3H-1,4-benzodiazepine A mixture of 2 g. (0.006 mole) of 7-nitro-1,3-dihydro- 5-(o-chlorophenyl) -2H-1,4-benzodiazepine-Z-thione, 1.50 g. (0.013 mole) of allyloxyamine hydrochloride and 1.29 g. of sodium bicarbonate in 70 ml. of ethanol was brought to reflux and kept at reflux for 10 hours. Nitrogen gas was bubbled through the solution. The solution was then evaporated to give a residue which was dissolved in 75 ml. of methylene chloride. The methylene chloride solution was filtered through activated charcoal and evaporated to dryness giving 1.5 g. of a yellow-orange compound which was crystallized from cyclohexane and ethyl acetate and Skellysole B hexanes to give a total of 1.1 g. of 2 [(allyloxy)amino]-7-nitro-5-(o-chlorophenyl)-3H- 1,4-benzodiazepine of melting point 178-180".

Analysis.Calcd. for C H ClN O (percent): C, 58.38; H, 4.05; N, 15.15; Cl, 9.46. Found (percent): C, 58.65; H, 4.31; N, 14.98; C], 9.44.

EXAMPLE 24 2- (allyl0xy)amin0] -5-(0-chl0r0phelzyl) 3H-1,4-benz0diazepine In the manner given in Example 5, a mixture of 1,3- dihydro 5 (o-chlorophenyl)-2H-1,4-benzodiazepine-2- thione, allyloxyamine hydrochloride, sodium bicarbonate, and methanol was refluxed to give 2-[(allyloxy)amino]- 5- (o-chlorophenyl) -3 H-1,4-benzodiazepine.

EXAMPLE 25 2-[ (allyl0xy)amin0] -5-(2,6-dichl0r0phenyl)- 3H-1,4-benz0diazepine In the manner given in Example 5 a mixture of 1,3- dihydro 5 (2,6-dichlorophenyl)-2H-l,4-benzodiazepine- 2-thione, allyloxyamine hydrochloride, sodium bicarbonate, and methanol was refluxed to give 2-[(allyloxy)- amino]-5-(2,6-dichlorophenyl)-3H-l,4-benzodiazepine.

1 1 EXAMPLE 26 In the manner given in Example 5, a mixture of 1,3- dihydro 5 (2,6-difluorophenyl)-2H-1,4-benzodiazepine- 2-thione, allyloxyamine hydrochloride, sodium bicarbonate, and methanol was refluxed to give 2-[(allyloxy)- amino]-5-(2,6-difiuoropheny1)-3H-1,4benzodiazepine.

EXAMPLE 27 2-[ (allyloxy amino] -5- (o-fluorophenyl) 3H ,4-benzdiazepine In the manner given in Example 5, a mixture of 1,3-dihydro 5 (o-fluorophenyl) 2H-1,4-benzodiazepine-2- thione, allyloxyamine hydrochloride, sodium bicarbonate, and methanol was refluxed to give 2[ (allyloxy)amino]-5- (o-fluorophenyl)-3H-1,4-benzodiazepine.

EXAMPLE 28 7,9-clichl0r0-2- (methoxyamino -5- (2,6-dichl0r0phenyl 3H ,4-benz0diazepine In the manner given in Example 1, a mixture of 7,9-dichloro 1,3 dihydro 5 (2,6-dichlorophenyl)-2H-1,4- benzodiazepine-Z-thione, methoxyamine hydrochloride, sodium bicarbonate, and methanol was refluxed to give 7,9 dichloro-Z-(methoxyamino)-5-(2,6-dichlorophenyl)- 3H-1,4-benzodiazepine.

EXAMPLE 29 In the manner given in Example 1, a mixture of 6,7- dicyano 1,3-dihydro-5-(m-nitrophenyl)-2H-1,4'benzodiazepine-Z-thione, ethoxyamine hydrochloride, and sodium bicarbonate was refluxed in methanol to give 6,7 -dicyano- 2 (ethoxyamino) 5 (m-nitrophenyl)-3H-1,4-benzodiazepine.

EXAMPLE 3O 2-(t-butoxyamina)-7,9-dichlor0-5-(2,6-dichl0r0phenyl 3H ,4-benz0diazepine In the manner given in Example 1, a mixture of 7,9-dichloro 1,3-dihydro-5- (2,6-dichlorophenyl)-2H-1,4-benzediazepine-Z-thione, S-butoxyamine hydrochloride, and sodium bicarbonate was refluxed in methanol to give 2- (t-butoxyamino) 7,9 dichloro-5-(2,6-dichlorophenyl)- 3H-1,4-benzodiazepine.

EXAMPLE 3 1 2- (propoxyamino) -6-methyl-7-br0mo-5-( p-methylphenyl) -3H-1,4-benz0diazepine In the manner given in Example 1, a mixture of 6- methyl 7-bromo-1,3-dihydro-5-(p-methylphenyD-ZH-1,4- benzodiazepine-Z-thione, propoxyamine hydrochloride and sodium bicarbonate was refluxed in methanol to give 2- (propoxyamino) 6-methyl-7-bromo5- (p-methylphenyl) 3H-1,4-benzodiazepine.

EXAMPLE 32 12 EXAMPLE 33 2-[3-(diethylamino)propoxyamino] -7,9-dicyan0-5-(2,4- dibromophenyl) 3H-1,4-benzadiazepine In the manner given in Example 1, a mixture of 1,3-dihydro 7,9-dicyano-5-(2,4-dibromophenyl)-2H-1,4-benzodiazepine-Z-thione, 3-(diethylamino)propoxyamine hydrochloride and sodium bicarbonate was refluxed in methanol to give 2- [3- (diethylamino propoxyamino]-7,9-dicyano-5- 2,4-dibromophenyl)-3H1,4-benzodiazepine.

EXAMPLE 34 2- (allyloxy amino-8-nitr0-5-(o -chlorophenyl)- 3H ,4-benz0diazepine In the manner given in Example 5, a mixture of 8- nitro 1,3 dihydro-5-(o-chlorophenyl)-2H-1,4-benzodiazepine-Z-thione, allyloxyamine hydrochloride, and sodium bicarbonate was refluxed in methanol to give 2-[(ally1- oxy)amino] 8 nitro-S- (o-chlorophenyl-3H-1,4-benzodiazepine.

EXAMPLE 35 2- (isopropoxyamino -7-chl'0r0-5- (2-chl0ro-4-metlzylphenyl)-3H-1,4-benzadiazepine In the manner given in Example 1, a mixture of 7- chloro 1,3 dihydro-S-(2-chloro-4-methylphenyl)-2H- 1,4 benzodiazepine 2 thione, isopropoxyamine hydrochloride, and sodium bicarbonate was refluxed in methanot to give 2 (isopropoxyamino) 7 chloro-S-(Z-chloro- S-methylphenyl) -3 H1,4-benzodiazepine.

EXAMPLE 3 6 2-[ (benzyloxy amin0]-6,8-dimethyl-5- (3,5-dieth0xyphenyl) -3H-1,4-benz0diazepine In the manner given in Example 1, a mixture of 6,8-dimethyl 1,3 dihydro 5 (3,5 diethoxyphenyl) 2H- 1,4 benzodiazepine 2 thione, benzyloxyamine hydrochloride, and sodium bicarbonate was refluxed in methanot to give 2-[(benzyloxy)amino]-6,8-dimethyl-5-(3,5- diethoxyphenyl) -3H- 1,4-benzodiazepine.

EXAM PLE 3 7 2[(allyloxy)amin01-7-ethyl-5-(o-butylphenyD-ZH- 1,4-benz0dz'azepine In the manner given in Example 5, a mixture of 1,3-dihydro 7 ethyl 5 (o-butylphenyl)-2H-l,4-benzodiazepine 2 thione, allyloxyamine hydrochloride and sodium bicarbonate was refluxed to give 2[(allyloxy) amino] 7 ethyl 5 (o-butylphenyl) 2H 1,4-benzodiazepine.

EXAMPLE 38 2-[ (allyloxy )amino]-7,8-dfpr0pyl-5-(o-nzethylthiophenyl -2H-1 ,4-benz0diazepine In the manner given in Example 5, a mixture of 1,3-dihydro-7,8-dipropyl 5 (o-methylthiophenyl) 2H 1,4- benzodiazepine 2 thione, allyloxyamine hydrochloride and sodium bicarbonate was refluxed to give 2-[(allyloxy)amino] 7,8 dipropyl 5 (o-methylthiophenyl) 2H 1,4 benzodiazepine.

EXAMPLE 39 -butylthio-Z- (ethoxyamino) -5- (p-pi'opoxyphenyl 2H-1 ,4-benzodiazepine In the manner given in Example 1, a mixture of 1,3-dihydro 6 butylthio 5 (P-propoxyphenyl)-2H-1,4- benzodiazepine 2 thione, ethoxyamine hydrochloride and sodium bicarbonate was refluxed to give o-butylthio- 2 (ethoxyamino) 5 (p-propoxyphenyl 2H 1,4- benzodiazepine.

13 EXAMPLE 40 In the manner given in Example 1, a mixture of 1,3-dihydro 7 bromo 9 methylthio 5 (3,5-difiuorophenyl) 2H 1,4 benzodiazepine 2 thione, allyloxyamine hydrochloride and sodium bicarbonate was refluxed to give 2 [(allyloxy)amino] 9 methylthio-7-bromo- 5 (3,5 diliuorophenyl) 2H 1,4 benzodiazepine.

EXAMPLE 41 9-isopr0pyl-7-nitro-2-[ (allyloxy amino] -5-[2,6- bis(ethylthi )phenyl] -2H-1,4-benz0diazepine In the manner given in Example 1, a mixture of 1,3-dihydro 9 isopropyl 7 nitro [2,6-bis(ethylthio) phenyl] 2H 1,4 benzodiazepine 2 thione, allyloxyamine hydrochloride and sodium carbonate was refluxed to give 2 [(allyloxy)amino] 5 [2,6 bis(ethylthio) phenyl] 2H 1,4-benzodiazepine.

In the manner given in the preceding examples, other 3H 1,4 benzodiazepines of Formula II are obtained by treating 2H 1,4 benzodiazepine 2 thiones of Formula I with an oxyamino compound H N-OR, wherein R is defined as above. Representative compounds of Formula II, thus obtained include:

2- allyloxyamino) -7-bromo-5-phenyl-3H- 1 ,4-benzodiazepine;

2-[ (3 -butenyloxy amino] -7-trifiuoromethyl-5- (o-chlorophenyl )3 H-1,4benzodiazepine;

2- (isopropoxyamino)-7-butyl-5-phenyl-3H-1,4-benzodiazepine;

2- (benzyloxyamino) -7-fluoro-5- (o-bromophenyl) -3H- 1,4-benzodiazepine;

2- (ethoxyamino) -7-ch1oro-5- (o-fiuorophenyl -3 H-1,4-

benzodiazepine;

2- (propoxyamino -7-cyano-5-phenyl-3H- 1 ,4-benzodiazepine;

2- (butoxyamino) -7-nitro-5-phenyl-3H-1 ,4-benzodiazepine;

Z-(isopropoxyamino) -5- (o-bromophenyl) -3H-1,4-benzodiazepine;

2- [3-( 1-piperidinyl)propoxyamino]-5-phenyl-3H-1,4-

benzodiazepine;

2- [2- dimethylamino) ethoxyamino] -5- o-fiuorophenyl) 3H-1,4-benzodiazepine;

2- allyloxyamino -7-nitro-S-phenyl-3H- 1 ,4-benzodiaze ine;

2-hydroxyamino-7-cyano-5- (o-bromophenyl) -3H-1,

benzodiazepine;

2-hydroxyamino6,7-difiuoro-5- 3 ,5 trifiuoromethyl phenyl] -3H-1,4-benzodiazepine;

2-benzyloxyamino-7,9-dicyano-5- 2,4-dibromophenyl 3 H-1,4-benzodiazepine;

2-b utoxyamino-6,7-dicyanc 5- m-nitrophenyl -3 H-1,4-

benzodiazepine;

2- allyloxy) amino] -7,9-dichloro-5- 2,6-dihclorophenyl -3 H-1,4-benzodiazepine;

2-[ crotyloxy) amino] -7,9-dichloro-5- 2,6-dichloropheny1)-3 H-1,4-benzodiazepine;

and the like.

Acid addition salts of compounds of Formula 111 are obtained by reacting the selected compound of Formula II with one or more equivalent of acid to get the desired acid addition salt. The reaction is carried out at zero to 25 C. in a solvent, for example, ether, ethyl acetate, anhydrous or aqueous methanol, ethanol, or isopropanol, and the solvent is thereupon evaporated. In this manner, pharmacologically acceptable acid addition salts, e.g., hydrochlorides, hydrobromides, sulfates, phosphates, acetates, propionates, tartrates, succinates, lactates, citrates, maleates, malates, phenylacetates, phenylpropionates, benzoates, cinnamates, salicylates, cyclohexanesulfamates,

pamoates, methanesulfonates and the like of Formula II compounds are obtained.

What is claimed is:

1. A 3H-1,4-benzodiazepine of the formula:

wherein R is selected from the group consisting of hydrogen, lower-alkyl of 1 to 4 carbon atoms, inclusive, loweralkenyl of 3 or 4 carbon atoms, benzyl, H CCOOH and (CH COOH and the esters thereof derived from an alkanol of 1 to 3 carbon atoms, inclusive, and

R5 2)uN in which n is 2 or 3 or together signify the pyrrolidino or piperidino radical; and wherein R R R and R are selected from the group consisting of hydrogen, lower alkoxy of 1 to 3 carbon atoms, inclusive, alkyl defined as above, alkylthio in which the alkyl group is defined as above, halogen, nitro, cyano and CF and the pharmacologically acceptable acid addition salts thereof.

2. A compound according to claim 1 wherein R is 7- chloro, R R and R are hydrogen and R is methyl and the compound is therefore 2-(methoxyamino)-7-chloro-5- phenyl-3H-1,4-benzodiazepine.

3. A compound according to claim 1 wherein R is 7- chloro, R R and R are hydrogen and R is benzyl and the compound is therefore 2-(benzyloxyamino)-7-chloro- 5-phenyl-3H-1,4-benzodiazepine.

4. A compound according to claim 1 wherein R is 7- chloro, R R and R are hydrogen and R is 2-(1-pyrrolidinyl)ethyl and the compound is therefore 2-[2-(1- pyrrolidinyDethoxyamino] 7 chloro-5-phenyl-3H-1,4- benzodiazepine.

5. A compound according to claim 1 wherein R is 7- chloro, R R and R are hydrogen and R is t-butyl and the compound is therefore 2-(t-butoxyamino)-7-chloro-5- phenyl-3H-1,4-benzodiazepine.

6. A compound according to claim 1 wherein R is 7- chloro, R R and R are hydrogen and R is allyl and the compound is therefore 2-(allyloxyamino)-7-chloro-5- phenyl-3H-1,4-benzodiazepine.

7. A compound according to claim 1 wherein R is 7- chloro, R R and R are hydrogen and R is 2-(diethylamino)ethyl and the compound is therefore 2-[2-diethy1- amino)ethoxyamino] 7 chloro 5-phenyl-3H-1,4-benzodiazepine.

8. A compound according to claim 1 wherein R is 7- chlor, R R and R are hydrogen and R is and the compound is therefore ethyl [(7-chloro-5-phenyl- 3H1 1,4-benzodiazepin-2-yl aminooxy] acetate.

9. A compound according to claim 1 wherein R is 7- chloro, R, R R and R are hydrogen and the compound is therefore 2-(hydroxyamino)-7-chloro-5-pheny1- 3H-1,4-benzodiazepine.

10. A compound according to claim 1 wherein R is 7- chloro, and R is o-chloro, R and R are hydrogen, and

1 R is allyl and the compound is therefore Z-(allyloxyamino) 7 chloro 5 (o-chlorophenyl)-3H-1,4-benzodiazepine.

11. A compound according to claim 1 wherein R is 7- chloro, and R is o-chloro, R and R are hydrogen and R is methyl and the compound is therefore Z-(methoxyamino) 7 chloro 5 (o-chlorophenyl)-3H-l,4-benzodiazepine.

12. A compound according to claim 1 wherein R is 7- nitro R and R are hydrogen and R is o-chloro and R is allyl and the compound is thus 2-[(allyloxy)amino]-7- nitro-S-(o-chlorophenyl)-3H-1,4-benzodiazepine.

13. A compound according to claim 1 wherein R R and R are hydrogen, R is o-chloro and R is allyl, and the compound is thus 2-[(allyloxy)amino-S-(o-chlorophenyl)-3H-1,4-benzodiazepine.

16 References Cited UNITED STATES PATENTS 10 ALTON D. ROLLINS, Primary Examiner U.S. C1. X.R.

71-88, 94, 95; 260-2393 D, 293.4 R, 293.4 A, 294.7 G,

UNTTED STATES PATENT OFFICE CER'HHCATE 0F CQRRECTIGN Patent No. 5, 9, 7 Dated Ma rch 97 Inventor(s) Jackson B Hester J F It is certified that error appears in the above-identified patent and that said Letters Patent are hereby corrected as shown below:

Column 2, l lne 51, for or R or R read or R and R l lne 52, for of 4 to 5" read of 4 or 5 l ine 58, for "oxylamine" read oxyami ne l ine 47, for to a l kenyl read of a l kenyl Column 5, l ine 29, For methoxyaml no-7" read methoxyamlno) 7- l lne 40, for al loy loxyam l no read a l lyloxyam no l ine 40, for 'chloropheny l 5H-" read ch l oropheny 1 )-5H- l ine 65, for dr led Fl shmea l read dried fl shmeal; Column 4, l lne 10, for "benzod lazepl ne2ones' read benzod iazepin-2ones l lne 45, For "1,5- ld i hydro read 1,5-dlhyd r0 l lne 55, for )2H-l .4-" read )-2H-1,4- Column 6, l lne 1, for "[21" read [2- (1- l lne 17, for 2- (Butoxyamlno" read 2- (t-Butoxyam'i no Column 7, l lne 54 For (e=54,560, read (e=54,560), Column 8, l ine 12, for 58 .750" read 38,750 l ine 55, for "2-methoxyamino)" reac 2- (methoxya ml no) l ine 69, For benzod l apl ne" read benzodlazepi ne l ine 75, for refluxed methanol" read refluxed in methanol l l ne 74, for "benzod lazeplne" read benzod l azeoin Column 8, l ine 9, for H-l ,4- read 5H-1,4-

me 55, for )2 1, read )2H1 ,4- l u ne 42, For

5phenyl" read 5phenyl l lne 65, For )5H-1,4-" read )-5'H1, 4- Column 10, l lne 1 for [7-" read (7 Column 11, l lne 54, for (thoxyamlno read (ethoxyaml no) Column 12, l ine 5, for )5H-1,4-" read )-5Hl,4- l lne 24 -For benzad laziepi ne" read benzod iazepine l lne 74, for propoxyphem -2H" read propoxyphenyl )2H- Column 15, l lne 58, for d i h l oropheny l read d i chlorophenyl l ine 6 for "equ l valent" read equ i va l ents Column 14, l ine 61, for "22 read 2- [24 Signed and sealed this 26th day of September 1972.

(SEAL) Attest:

EDWARD PLJFLETCHER,JRo ROBERT GOTTSGHALK Attesting Officer Commissioner of Patents ORM PO-IOSO (IO-69) USCOMM-DC 603/6- 59 .5. GOVERNMENT PQINTING OFFICE: I959 O-J5f 334 

